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Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells

Porcine reproductive and respiratory syndrome is an infectious disease that causes serious economic losses to the swine industry worldwide. To better understand the pathogenesis of the porcine reproductive and respiratory syndrome virus (PRRSV), three PRRSV strains with different molecular markers a...

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Autores principales: Chen, Zhi, Liu, Shaoning, Zhang, Shujin, Zhang, Yuyu, Yu, Jiang, Sun, Wenbo, Chen, Lei, Du, Yijun, Wang, Jinbao, Li, Yubao, Wu, Jiaqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177479/
https://www.ncbi.nlm.nih.gov/pubmed/30302013
http://dx.doi.org/10.1038/s41598-018-32984-0
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author Chen, Zhi
Liu, Shaoning
Zhang, Shujin
Zhang, Yuyu
Yu, Jiang
Sun, Wenbo
Chen, Lei
Du, Yijun
Wang, Jinbao
Li, Yubao
Wu, Jiaqiang
author_facet Chen, Zhi
Liu, Shaoning
Zhang, Shujin
Zhang, Yuyu
Yu, Jiang
Sun, Wenbo
Chen, Lei
Du, Yijun
Wang, Jinbao
Li, Yubao
Wu, Jiaqiang
author_sort Chen, Zhi
collection PubMed
description Porcine reproductive and respiratory syndrome is an infectious disease that causes serious economic losses to the swine industry worldwide. To better understand the pathogenesis of the porcine reproductive and respiratory syndrome virus (PRRSV), three PRRSV strains with different molecular markers and virulence were used to infect MARC-145 cells. A total of 1804 proteins were identified, and 233 altered proteins and 72 signaling pathways involved in the proteomic profiling of virus-infected MARC-145 cells increased with the virulence of the PRRSV strain. The three types of viral strains shared a common pathway—the electron transport reaction in mitochondria—in the infected-MARC-145 cells. Moreover, the antisense pathway was the most variable of all significant signaling pathways for the highly virulent SX-1 strain, indicating that this unique pathway may be connected to the high virulence of the SX-1 strain. Our study is the first attempt to provide a proteome profile of MARC-145 cells infected with PRRSV strains with different virulence, and these findings will facilitate a deep understanding of the interactions between this virus and its host.
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spelling pubmed-61774792018-10-12 Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells Chen, Zhi Liu, Shaoning Zhang, Shujin Zhang, Yuyu Yu, Jiang Sun, Wenbo Chen, Lei Du, Yijun Wang, Jinbao Li, Yubao Wu, Jiaqiang Sci Rep Article Porcine reproductive and respiratory syndrome is an infectious disease that causes serious economic losses to the swine industry worldwide. To better understand the pathogenesis of the porcine reproductive and respiratory syndrome virus (PRRSV), three PRRSV strains with different molecular markers and virulence were used to infect MARC-145 cells. A total of 1804 proteins were identified, and 233 altered proteins and 72 signaling pathways involved in the proteomic profiling of virus-infected MARC-145 cells increased with the virulence of the PRRSV strain. The three types of viral strains shared a common pathway—the electron transport reaction in mitochondria—in the infected-MARC-145 cells. Moreover, the antisense pathway was the most variable of all significant signaling pathways for the highly virulent SX-1 strain, indicating that this unique pathway may be connected to the high virulence of the SX-1 strain. Our study is the first attempt to provide a proteome profile of MARC-145 cells infected with PRRSV strains with different virulence, and these findings will facilitate a deep understanding of the interactions between this virus and its host. Nature Publishing Group UK 2018-10-09 /pmc/articles/PMC6177479/ /pubmed/30302013 http://dx.doi.org/10.1038/s41598-018-32984-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Zhi
Liu, Shaoning
Zhang, Shujin
Zhang, Yuyu
Yu, Jiang
Sun, Wenbo
Chen, Lei
Du, Yijun
Wang, Jinbao
Li, Yubao
Wu, Jiaqiang
Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells
title Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells
title_full Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells
title_fullStr Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells
title_full_unstemmed Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells
title_short Porcine Reproductive and Respiratory Syndrome Virus strains with Higher Virulence Cause Marked Protein Profile Changes in MARC-145 Cells
title_sort porcine reproductive and respiratory syndrome virus strains with higher virulence cause marked protein profile changes in marc-145 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177479/
https://www.ncbi.nlm.nih.gov/pubmed/30302013
http://dx.doi.org/10.1038/s41598-018-32984-0
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